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FoodRecallWatch
Recalls & Withdrawals

FDA Food Recall

A voluntary or mandatory action by a firm to remove a food product from the market when it may be unsafe or mislabeled.

What It Means

An FDA food recall is the process by which a food manufacturer, distributor, or importer removes a product from the market, or corrects a problem with a product, because it violates laws enforced by the U.S. Food and Drug Administration. The vast majority of food recalls are initiated voluntarily by the company responsible for the product, although the FDA has the authority to mandate recalls when necessary. The recall process begins when a problem is identified, either through the company's own quality control, consumer complaints, FDA inspections, or laboratory testing. The FDA then evaluates the health hazard posed by the product and assigns a classification (Class I, II, or III) based on the severity of the risk. Once a recall is initiated, the recalling firm is responsible for notifying its distribution chain, issuing public notifications, and removing the product from shelves. The FDA publishes recall information through its Enforcement Reports, press releases, and the openFDA database. Food recalls can be triggered by a wide range of issues including pathogen contamination, undeclared allergens, foreign object contamination, chemical contamination, or labeling violations. Understanding how FDA recalls work helps consumers make informed decisions about the food they purchase and consume.

Related Terms

Frequently Asked Questions

What does FDA Food Recall mean?

A voluntary or mandatory action by a firm to remove a food product from the market when it may be unsafe or mislabeled.

Why is FDA Food Recall important for food safety?

An FDA food recall is the process by which a food manufacturer, distributor, or importer removes a product from the market, or corrects a problem with a product, because it violates laws enforced by the U.S. Food and Drug Administration. The vast majority of food recalls are initiated voluntarily by...

this entity is one of the U.S. FDA food, drug, and device recalls concepts that recurs across this site. The definition above is the technical answer; the paragraphs below add the practical context for how the concept connects to the the FDA openFDA enforcement-report API data behind every per-entity page on the site.

In the the FDA openFDA enforcement-report API data, this concept shapes one or more of the fields that drive the per-entity grades and rankings on this site. The methodology page describes which fields feed into which output; this glossary entry documents the underlying term.

Source: FDA Recalls, Market Withdrawals and Safety Alerts, 2026.